Variant DetailsVariant: nssv1150652Internal ID | 15529087 | Landmark | | Location Information | | Cytoband | 19q13.32 | Allele length | Assembly | Allele length | hg38 | 14744 | hg19 | 14744 | hg18 | 14744 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | nsv579903 | Supporting Variants | | Samples | HGDP00734 | Known Genes | CARD8, LOC100505812 | 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) | nssv1150652
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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