Variant DetailsVariant: nssv1141450Internal ID | 15647950 | Landmark | | Location Information | | Cytoband | 9q33.3 | Allele length | Assembly | Allele length | hg38 | 86218 | hg19 | 86218 | hg18 | 86218 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv615342 | Supporting Variants | | Samples | | Known Genes | ANGPTL2, RALGPS1 | Method | SNP array | Analysis | Illumina SNP array copy number analysis | Platform | Not reported | Comments | | Reference | Cooper_et_al_2011 | Pubmed ID | 21841781 | Accession Number(s) | nssv1141450
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|