Variant DetailsVariant: dgv11246n54Internal ID | 20144670 | Landmark | | Location Information | | Cytoband | 7p15.1 | Allele length | Assembly | Allele length | hg38 | 771 | hg19 | 771 | hg18 | 771 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv606477, nsv606476, nsv606480, nsv606474, nsv606473, nsv606475 | Samples | | Known Genes | CREB5 | 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) | dgv11246n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 192 | Observed Complex | 0 | Frequency | n/a |
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