Variant DetailsVariant: nsv569071Internal ID | 16009794 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 251627 | hg19 | 251627 | hg18 | 251627 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv4468n54 | Supporting Variants | nssv840272, nssv840273, nssv840270, nssv840268, nssv840274, nssv840269, nssv840271 | Samples | | Known Genes | GOLGA8B, MIR1233-1, MIR1233-2, MIR5588 | 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) | nsv569071
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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