Variant DetailsVariant: dgv12879n54Internal ID | 20146303 | 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 | M | Merged Variants | | Supporting Variants | nsv615372, nsv615370 | 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) | dgv12879n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 2 | Observed Complex | 0 | Frequency | n/a |
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