Angelman Syndrome: (15q11q13) FISH Analysis
Test code: CASS
TAT: 28 days
A cytogenetic test used to identify identify deletions or duplications in chromosome region 15q11q13.
Chromosomes
Chromosome 14 UPD Analysis
Test code: DC14
TAT: 21 days
Prenatal Samples Accepted
A comparative analysis between the proband and parental samples for markers on chromosome 14.
Chromosome 15 UPD Analysis
Test code: DC15
TAT: 21 days
Prenatal Samples Accepted
A comparative analysis between the proband and parental samples for markers on chromosome 15.
Chromosome 7 UPD Analysis
Test code: DC07
TAT: 21 days
Prenatal Samples Accepted
A comparative analysis between the proband and parental samples for markers on chromosome 7.
Chromosome Analysis (Bone Marrow)
Test code: CBMR
TAT: 10 days
A cytogenetic test on bone marrow, used in assessing remission or relapse of malignancy in individuals with myelodysplastic syndrome, acute myeloid leukemia, acute lymphoblastic leukemia, or lymphoproliferative disorders.
Chromosome Analysis (Stimulated/Unstimulated Blood)
Test code: CBSU
TAT: 10 days
A cytogenetic test on stimulated/unstimulated cultures, used in assessing remission or relapse of malignancy and/or to determine the presence or absence of abnormal clones.
Chromosome Analysis, High Resolution (Blood)
Test code: CBHR
TAT: 21 days
A cytogenetic test used to detect subtle or cryptic chromosome structural rearrangements at a high resolution.
Chromosome Analysis, High Resolution; Rule Out Mosaic (Blood)
Test code: CBHM
TAT: 21 days
A cytogenetic test used to detect subtle chromosomal structural rearrangements at a higher resolution and lower level of mosaicism.
Chromosome Analysis, Routine (Amniotic Fluid)
Test code: CARO
TAT: 14 days
A cytogenetic test used to detect chromosomal abnormalities.
Chromosome Analysis, Routine (Blood)
Test code: CBRO
TAT: 21 days
A cytogenetic test used to detect chromosomal abnormalities.
Chromosome Analysis, Routine (Chorionic Villus Sampling (CVS))
Test code: CCVR
TAT: 14 days
A cytogenetic test used to detect chromosomal abnormalities.
Chromosome Analysis, Routine (POC)
Test code: CCRP
TAT: 6 weeks
A cytogenetic test used to detect imbalances of genetic material that may explain the cause of a pregnancy loss.
Chromosome Analysis, Routine (Solid Tissue)
Test code: CSTR
TAT: 6 weeks
A cytogenetic test used to detect chromosomal abnormalities.
Chromosome Analysis, Routine; Rule Out Mosaic (Amniotic Fluid)
Test code: CARM
TAT: 14 days
A cytogenetic test used to detect chromosomal abnormalities at a larger count to assess for mosaicism.
Chromosome Analysis, Routine; Rule Out Mosaic (Blood)
Test code: CBRM
TAT: 21 days
A cytogenetic test used to detect chromosomal abnormalities at larger count.
Chromosome Analysis, Routine; Rule Out Mosaic (POC)
Test code: CPLM
TAT: 6 weeks
A cytogenetic test used to detect imbalances of genetic material that may explain the cause of a pregnancy loss.
Chromosome Analysis, Routine; Rule Out Mosaic (Solid Tissue)
Test code: CTRM
TAT: 6 weeks
A cytogenetic test used to detect chromosomal abnormalities at a larger count to assess for mosaicism.
Chromosome Analysis, Routine; Short Study (Amniotic Fluid)
Test code: CASH
TAT: 14 days
A cytogenetic test used to detect chromosomal abnormalities.
Chromosome Analysis, Routine; Short Study (Blood)
Test code: CBSS
TAT: 21 days
A cytogenetic test used to detect chromosomal abnormalities.
Chromosome Analysis, Routine; Short Study (Chorionic Villus Sampling (CVS))
Test code: CCSS
TAT: 14 days
A cytogenetic test used to detect chromosomal abnormalities.
Chromosome Analysis, Routine; Short Study (POC)
Test code: CPLS
TAT: 6 weeks
A cytogenetic test used to detect chromosomal abnormalities.
Chromosome Analysis, Routine; Short Study (Solid Tissue)
Test code: CTSS
TAT: 6 weeks
A cytogenetic test used to detect chromosomal abnormalities.
DiGeorge/VCF: (22q11.2) FISH Analysis
Test code: C22Q
TAT: 28 days
A cytogenetic test used to identify deletions or duplications in chromosome region 22q11.2.
Disorders of Sexual Development: FISH Panel, Routine (Buccal) (includes SRY/Xcen & X/Y dual assay probes)
Test code: CBSR
TAT: 28 days
A cytogenetic test intended for patients with a diagnosis or clinical suspicion of a disorder of sexual development.
Disorders of Sexual Development: FISH Panel, Routine (includes SRY/Xcen & X/Y dual assay probes)
Test code: CXYA
TAT: 28 days
A cytogenetic test intended for patients with a diagnosis or clinical suspicion of a disorder of sexual development.
A cytogenetic test intended for patients with a diagnosis or clinical suspicion of a disorder of sexual development.
Disorders of Sexual Development: FISH Panel, Rule Out Mosaic (includes SRY/Xcen & X/Y dual assay probes)
Test code: CXYM
TAT: 28 days
A cytogenetic test intended for patients with a diagnosis or clinical suspicion of a disorder of sexual development.
EpiSign Complete
Test code: DEPI
TAT: 28 days
EpiSign Complete is the first clinical assay validated to detect unique epigenetic signatures and methylation abnormalities for over 90 recognized genetic conditions.
EpiSign Variant
Test code: DEPT
TAT: 28 days
EpiSign Variant is a targeted review of methylation data intended to resolve variants of uncertain clinical signficance in genes with a known epigenetic signature.
Prader-Willi Syndrome: (15q11q13) FISH Analysis
Test code: CPWS
TAT: 28 days
A cytogenetic test used to identify identify deletions or duplications in chromosome region 15q11q13.
Trisomy 13 FISH, Rule Out Mosaic (Buccal)
Test code: CT13
TAT: 28 days
A cytogenetic test used to detect varying degrees of mosaicism in chromosome 13 aneuploidy.
Trisomy 18 FISH, Rule Out Mosaic (Buccal)
Test code: CT18
TAT: 28 days
A cytogenetic test used to detect varying degrees of mosaicism in chromosome 18 aneuploidy.
Trisomy 21 FISH, Rule Out Mosaic (Buccal)
Test code: CT21
TAT: 28 days
A cytogenetic test used to detect varying degrees of mosaicism in chromosome 21 aneuploidy.
Trisomy FISH Screen (13,18,21,X,Y) (Amniotic Fluid)
Test code: CTAF
TAT: 4 days
A cytogenetic test used to identify aneuploidies in chromosomes 13, 18, 21, X, and Y.
Trisomy FISH Screen (13,18,21,X,Y) (Blood)
Test code: CANE
TAT: 28 days
A cytogenetic test used to identify aneuploidies in chromosomes 13, 18, 21, X, and Y.
Trisomy FISH Screen (13,18,21,X,Y) (Chorionic Villus Sampling (CVS))
Test code: CTCV
TAT: 4 days
A cytogenetic test used to identify aneuploidies in chromosomes 13, 18, 21, X, and Y.