Deletion-Duplication analysis of Multiple Genes
Clinical Genetic Test
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offered by
GTR Test Accession: Help GTR000593846.1
INHERITED DISEASE
Registered in GTR: 2021-08-24
Last annual review date for the lab: 2024-03-25 LinkOut
At a Glance
Diagnosis
Hereditary disease
AKR1C2 (10p15.1); AKR1C4 (10p15.1); AR (Xq12); CBX2 (17q25.3); DHH (12q13.12) more...
Molecular Genetics - Deletion/duplication analysis: Next-Generation (NGS)/Massively parallel sequencing (MPS)
Not provided
Not provided
Not provided
Ordering Information
Test Order Code: Help
906
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
Decline to answer
Post-test genetic counseling required: Help
Decline to answer
Recommended fields not provided:
Conditions Help
Total conditions: 1
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 20
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Deletion/duplication analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis
Recommended fields not provided:
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Specificity for exon-level arrayCGH is >99.9% and the analytical sensitivity ranges from 95.5% - 99.9%. Assessment of exon-level copy number events is dependent on the inherent sequence properties of the targeted regions, including shared homology and exon size.
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
Recommended fields not provided:
Regulatory Approval
FDA Review: Help
Not provided
Additional Information
Practice guidelines:
Consumer resources:

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