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Osteogenesis Imperfecta Panel, Comprehensive
Clinical Genetic Test
Help
offered by
CNH Molecular Diagnostics Laboratory
GTR Test Accession: Help GTR000569562.1
INHERITED DISEASEDYSMORPHOLOGYMUSCULOSKELETAL ... View more
Registered in GTR: 2019-11-15
View version history
Last annual review date for the lab: 2024-10-28 LinkOut
At a Glance
Test purpose: Help
Diagnosis
Conditions (23): Help
Adult hypophosphatasia; Bruck syndrome 1; Bruck syndrome 2 more...
Genes (12): Help
ALPL (1p36.12); BMP1 (8p21.3); COL1A1 (17q21.33); COL1A2 (7q21.3); CRTAP (3p22.3) more...
Methods (1): Help
Molecular Genetics - Sequence analysis of the entire coding region: 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
CNH Molecular Diagnostics Laboratory
View lab's website
Test Order Code: Help
MO0042
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: 23
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 12
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
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 analytical sensitivity of NGS sequencing is estimated to be > 99% at detecting single nucleotide events. It will not reliably detect deletions greater than 20 base pairs, insertions or rearrangements greater than 10 base pairs, or low-level mosaicism.
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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