Variant DetailsVariant: nsv569577Internal ID | 16010300 | Landmark | | Location Information | | Cytoband | 15q21.3 | Allele length | Assembly | Allele length | hg38 | 142761 | hg19 | 142761 | hg18 | 142761 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1149221 | Samples | HGDP01023 | Known Genes | LOC145783, TCF12 | 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) | nsv569577
| Frequency | Sample Size | 17421 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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