Variant DetailsVariant: nsv605939Internal ID | 16046662 | Landmark | | Location Information | | Cytoband | 7p22.1 | Allele length | Assembly | Allele length | hg38 | 658093 | hg19 | 658092 | hg18 | 658092 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nssv1155132, nssv1155128, nssv1155129, nssv1155131, nssv1155127, nssv1155130 | Samples | HGDP01001, HGDP01014, HGDP01016, HGDP01003, HGDP01017, HGDP01018 | Known Genes | SDK1 | 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) | nsv605939
| Frequency | Sample Size | 17421 | Observed Gain | 6 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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