Submitter |
RCV |
SCV |
Clinical significance |
Condition |
Last evaluated |
Review status |
Method |
Comment |
Baylor Genetics |
RCV000767675 |
SCV000898297 |
likely pathogenic |
not provided |
2018-11-01 |
criteria provided, single submitter |
clinical testing |
This CNV was detected in a symptomatic patient referred for CMA testing, but consent was not obtained to report individual clinical features |
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