Variant DetailsVariant: nssv1155227Internal ID | 15528178 | Landmark | | Location Information | | Cytoband | 7q32.1 | Allele length | Assembly | Allele length | hg38 | 76166 | hg19 | 76166 | hg18 | 76166 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv608403 | Supporting Variants | | Samples | HGDP00602 | Known Genes | ATP6V1F, CCDC136, FLNC, KCP, LOC100130705 | 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) | nssv1155227
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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