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Hereditary High Risk Breast Cancer Panel
Clinical Genetic Test
Help
offered by
Baylor Genetics
GTR Test Accession: Help GTR000553676.3
INHERITED DISEASECANCERINHERITED DISEASE SUSCEPTIBILITY ... View more
Last updated in GTR: 2019-07-01
View version history
Last annual review date for the lab: 2023-07-21 LinkOut
At a Glance
Test purpose: Help
Diagnosis
Conditions (34): Help
Breast-ovarian cancer, familial, susceptibility to, 1; Adrenocortical carcinoma, hereditary; Basal cell carcinoma, susceptibility to, 7; ...
Genes (7): Help
BRCA1 (17q21.31), BRCA2 (13q13.1), CDH1 (16q22.1), PALB2 (16p12.2), PTEN (10q23.31), ...
Methods (2): Help
Molecular Genetics - Deletion/duplication analysis: Next-Generation (NGS)/Massively parallel sequencing (MPS); ...
Target population: Help
Not provided
Clinical validity: Help
Not provided
Clinical utility: Help
Not provided
Ordering Information
Offered by: Help
Baylor Genetics
View lab's website
Test Order Code: Help
23000
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:
How to Order, Specimen source, Lab contact for this test, Contact policy, Test strategy, Test development
Conditions Help
Total conditions: 34
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 7
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 2
Method Category Help
Test method Help
Instrument *
Deletion/duplication analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
Sequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis
Recommended fields not provided:
Clinical validity, Clinical utility, Target population, What is the protocol for interpreting a variation as a VUS?, Is research allowed on the sample after clinical testing is complete?, Sample negative report, Sample positive report
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
The sequence (NGS) analytical validity for SNV is >99% sensitivity, >99% specificity, >99% accuracy. The deletion/duplication analytical validity for CNV is higher than 99.9% sensitivity, >99% specificity, >99% accuracy to detect one exon or greater deletions and two exon or greater insertion, LOD standard deviation over 0.12 or coverage < … View more
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
Recommended fields not provided:
Test Confirmation, Assay limitations, Description of internal test validation method, Citations for Analytical validity, PT Provider, Description of PT method, Major CAP category, CAP category, CAP test list
Regulatory Approval
FDA Review: Help
Not provided
Additional Information

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