Key Information

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).

Chromosome 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

  • The preferred sample type is 3-4 ml of peripheral blood collected in an EDTA (purple top) tube. Extracted DNA and saliva are also accepted for this test. Blood and saliva kits are available by request.
  • Send approximately 5µg of extracted DNA at a requested concentration of 90-130 ng/µl.
  • Saliva samples must be submitted in an approved saliva kit.
  • This test requires a sample on the proband and both parents for complete analysis.

Transport Instructions

  • The specimen should be kept at room temperature and delivered via overnight shipping. If shipment is delayed by one or two days, the specimen should be refrigerated and shipped at room temperature. Do not freeze the specimen. Samples collected on Friday can be safely designated for Monday delivery.
  • Extracted DNA should be sent at room temperature via overnight delivery.
  • Saliva is stable at room temperature and can be delivered via overnight or ground shipping.

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

  • Amniotic Fluid: Direct amniotic fluid will be accepted for analysis given there is sufficient volume for back-up culture to be established. A back-up culture at a reference lab OR Greenwood lab is required. Additional charges may apply if cell culture is required after receipt of the sample. If sending direct fluid for molecular analysis only, 10-20 ml of amniotic fluid is requested. Chromosome studies will require an additional 10-15 ml of fluid.
  • Chorionic Villi Sample (CVS): 10-50 mg of chorionic villi is requested in a sterile tube with CVS media. Direct testing on CVS is not available; an additional 1-3 weeks may be needed for cultures to grow.
  • Cultured amniocytes/CVS: 2x T25 confluent flasks
  • A maternal sample is required, and accepted sample types include blood, saliva, and extracted DNA. Please refer to the specimen requirements above for more information.

Prenatal Transport Instructions

  • Amniotic fluid should be kept at room temperature; do not freeze or refrigerate. Specimen should be sent by courier or overnight mail to arrive at the laboratory the next day.
  • CVS and cultured amniocytes should be kept at room temperature; do not freeze or refrigerate. Specimen should be sent by courier or overnight mail to arrive at the laboratory the next day. FedEx is preferred.
  • Please refer to the transport instructions above for sending the maternal sample.

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