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Chromosome 22q11.2 microduplication syndrome, 608363, Autosomal dominant, Isolated cases (22q11.2 … see more Chromosome 22q11.2 microduplication syndrome, 608363, Autosomal dominant, Isolated cases (22q11.2 microduplication syndrome) (440)  see less
Clinical Genetic Test
Help
offered by
Intergen
GTR Test Accession: Help GTR000585323.1
INHERITED DISEASE
Registered in GTR: 2020-05-19
View version history
Last annual review date for the lab: 2024-11-15 LinkOut
At a Glance
Test purpose: Help
Diagnosis
Conditions (1): Help
Chromosome 22q11.2 microduplication syndrome
Chromosomal regions/ Mitochondria (1): Help
22q11.2
Methods (1): Help
Molecular Genetics - Deletion/duplication analysis: Microarray
Target population: Help
Chromosome 22q11.2 microduplication syndrome, 608363, Autosomal dominant, Isolated cases (diagnosis/ …
Clinical validity: Help
Not provided
Clinical utility: Help
Not provided
Ordering Information
Offered by: Help
Intergen
View lab's website
Test Order Code: Help
3280
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: 1
Condition/Phenotype Identifier
Test Targets
Chromosomal regions/Mitochondria Help
Total chromosomal regions/mitochondria: 1
Chromosomal region/Mitochondrion Associated condition
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Deletion/duplication analysis
Microarray
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis
Target population: Help
Chromosome 22q11.2 microduplication syndrome, 608363, Autosomal dominant, Isolated cases (diagnosis/ clinical suspition/ etiology investigation/ classification)
Recommended fields not provided:
Clinical validity, Clinical utility, 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
Array CGH test has 99% sensitivity and 99% specificity.
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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