Variant DetailsVariant: nsv561618Internal ID | 16002341 | Landmark | | Location Information | | Cytoband | 13q14.2 | Allele length | Assembly | Allele length | hg38 | 1613873 | hg19 | 1613873 | hg18 | 1613873 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1176446 | Samples | HGDP00539 | Known Genes | DLEU1, DLEU2, DLEU7, DLEU7-AS1, FAM124A, GUCY1B2, INTS6, INTS6-AS1, KCNRG, LINC00371, MIR15A, MIR16-1, MIR3613, MIR5693, RNASEH2B, RNASEH2B-AS1, SERPINE3, SPRYD7, ST13P4, TRIM13 | 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) | nsv561618
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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