Deletion / Duplication
New York
Approved
Clinical Utility
- To evaluate for deletions in genes associated with disorders for which haploinsufficiency is a known mechanism of disease.
- To evaluate for deletions or duplications when a single sequence variant has been identified in a gene associated with an autosomal recessive disorder.
- Deletion/duplication analysis by ExonArrayDx may be requested for a single gene (test code 906) or for a custom panel of up to 20 genes (test code 703).
Test Code
906
CPT Codes*
Varies by Gene
ABN Required
No
Turnaround Time**
3-4 weeks
Preferred Specimen
Alternative Specimen
*The CPT codes provided are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
**Turnaround times are estimates and begin once the sample(s) begin processing at the GeneDx lab and could be extended in situations outside GeneDx’s control.
Test Documents
Billing
Targeted Variant Testing