Chromosome 15
Chromosome 15 UPD Analysis
Key Information
Lab:
TAT:
21 days
Price:
$500
CPT Code(s):
81402
Test Code:
DC15
Prenatal Samples Accepted
Chromosome 15 UPD Analysis
Chromosome 15 uniparental disomy (UPD) analysis is used to determine if an individual’s genetic constitution reflects a contribution from both parents or only one parent (UPD). This test requires samples from both parents and can confirm a diagnosis of Angelman syndrome (maternal UPD 15) or Prader-Willi syndrome (paternal UPD 15).
Angelman syndrome, Prader-Willi syndrome
Technical Information
UPD causes approximately 25% of cases of Prader-Willi syndrome and approximately 7% of cases of Angelman syndrome. Segmental UPD may not be detected. Please provide coordinates prior to sending the sample for any region with absence of heterozygosity (AOH) to confirm that we have markers to cover the region of interest.
Specimen Requirements
Transport Instructions
Prenatal Testing Information
Prenatal diagnosis is available if there is a translocation in a parent and/or the fetus increasing the risk for UPD. Additional fees for cell culture may apply. Maternal cell contamination studies are not required for prenatal UPD analysis. Contact the laboratory prior to sending a prenatal specimen.
Prenatal Specimen Requirements
Prenatal Transport Instructions
Connect With Our Experts
Call 1-800-473-9411 to speak with our team of laboratory genetic counselors for questions or additional information.
Robin Fletcher, MS, CGC
Falecia Thomas, MS, CGC
Alex Finley, MS, CGC
