Comprehensive DFNB1 and STRC Panel
- GTR Test IDHelpEach Test is a specific, orderable test from a particular laboratory, and is assigned a unique GTR accession number. The format is GTR00000001.1, with a leading prefix 'GTR' followed by 8 digits, a period, then 1 or more digits representing the version. When a laboratory updates a registered test, a new version number is assigned.: GTR000591223.1
- Last updated: 2022-08-23
- Annual Review past due read more
- Test version history
- 591223.1, last updated: 2022-08-23
Clinical testHelpIn the U.S., clinical tests must be performed under CLIA certification. When a lab uses the same methods for a test in both clinical and research settings, the test appears as two separate GTR records. for Hereditary hearing loss and deafness
Offered by Laboratory for Molecular Medicine
Overview
Test name
HelpThe name the laboratory assigns the test. Used as the default title of the page specific to the test.Comprehensive DFNB1 and STRC Panel (DFNB1 and STRC)
This is a clinical test intended for HelpPurposes or indications for the test. Lab-provided.: Diagnosis
Click Indication tab for more information.
Order URL HelpLink to the laboratory webpage with information about how to order this test. Please note that clicking on this link will open a new tab in your internet browser.: http://personalizedmedicine.partners.org/Laboratory-For-Molecular-Medicine/Ordering/Default.aspx
Specimen source
Methodology
HelpThe assay's major method category (biochemical, cytogenetic or molecular genetics); method category (i.e. enzyme assay, chromosome breakage studies, targeted mutation analysis); methodology (i.e. the name of the method used) and instruments used when performing this test.- Molecular Genetics
- CSequence analysis of the entire coding region
- Next-Generation (NGS)/Massively parallel sequencing (MPS)
- Illumina NextSeq 550 Mid Output Kit
Not provided
Clinical validity
HelpHow consistently and accurately the test detects or predicts the intermediate or final outcomes of interest. Lab-provided.Not provided
- NICE, 2019Cochlear implants for children and adults with severe to profound deafness (2019 Update)
- ACMG ACT Sheet, 2018Newborn Screening ACT Sheet (Congenital Hearing Loss >30db)
- ACMG ACT Sheet, 2010American College of Medical Genetics ACT SHEET, Congenital Hearing Loss, 2010
- ACMG Algorithm, 2009American College of Medical Genetics Algorithm, Hearing Loss, 2009
- NICE, 2009National Institute for Health and Clinical Excellence, Cochlear implants for children and adults with severe to profound deafness, 2009 [See 2019 Update, TA566]
- ACMG Algorithm, 2009American College of Medical Genetics ACT SHEET, Newborn Screening ACT Sheet Algorithm, Congenital Hearing Loss, 2009
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