Casandra
Casandra Test Code QD21853Version 1 (DRAFT)
Performing Lab
FISH, Prader‑Willi/Angelman Syndrome
Also known as: Prader/Willi, Angelman Syndrome
Clinical Use
Order TestUse
This test is used to detect microdeletions of chromosome 15q11–q13 associated with Prader‑Willi syndrome using fluorescence in situ hybridization (FISH).
Special Instructions
Not provided.
Limitations
Not FDA‑cleared or approved; validated under CLIA and used for clinical purposes only. (No other limitations explicitly provided.)
Test Details
Methodology
Chromosomal / Cytogenetics (FISH)
Biomarkers
Unknown CNV
Copy Number RegionFISH
Copy Number Alteration • Categorical (e.g., Positive / Negative / Indeterminate)
Result Turnaround Time
14 days
Related Documents
For more information, please review the documents below
Specimen Requirements
Specimen
Whole Blood
Volume
5 mL preferred, 1 mL minimum
Minimum Volume
1 mL
Container
sodium heparin (green‑top) tube; also acceptable: royal blue‑top or tan‑top sodium heparin
Collection Instructions
Clinical history and reason for referral required with test order.
Stability Requirements
| Temperature | Period |
|---|---|
| Room Temperature | Specimen viability decreases during transit; do not freeze; do not reject |
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