Variant DetailsVariant: nssv1176498Internal ID | 15507991 | Landmark | | Location Information | | Cytoband | 9q34.11 | Allele length | Assembly | Allele length | hg38 | 93176 | hg19 | 93176 | hg18 | 93176 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv615370 | Supporting Variants | | Samples | 1780862275_A | Known Genes | CDK9, ENG, FPGS, MIR2861, MIR3960, SH2D3C, TOR2A, TTC16 | 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) | nssv1176498
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
|
|