Versiti LabsTest Menu
Order Code: 1288
VWD Type 2N Sequence Analysis
Test Information
Sequence analysis of VWF exons 17-21 and 24-27 detects germline variants associated with type 2N von willebrand disease (VWD). USA test status: This is a laboratory developed test (LDT).
Also Known As
- Von Willebrand Disease
- VWD
Test Type
Genetic Test
Sample Notes
EDTA Whole Blood, EDTA Bone Marrow, DNA, Buccal Swabs, Amniotic Fluid, Cultured Amniocytes, Direct or Cultured CVS, ACDA Whole Blood, ACDB Whole Blood, Na Heparin Whole Blood
Requested Volume
3-5 mL EDTA Whole Blood or Bone Marrow (lavender top), 3-4 Buccal Swabs, >=1 ug DNA at >=50 ng/uL, 7-15 mL Amniotic Fluid, 5-10 mg CVS, 2-T25 flasks cultured amniocytes or CVS (2x10^6 minimum)
Minimum / Pediatric Volume
Fetal: Call Laboratory; Parental/Patient: 2 mL EDTA whole blood
Shipping Information
Room Temperature or Refrigerated
CPT Codes
- 81405
Method
Capture Hybridization and Next Generation Sequencing with supplementary PCR and Sanger sequencing for quality and coverage.
Turnaround Time
21 days
New York State Approval
Yes
DEX Z-Code™
Yes, visit app.dexzcodes.com