Variant DetailsVariant: esv3621518Internal ID | 6661697 | Landmark | | Location Information | | Cytoband | 9q32 | Allele length | Assembly | Allele length | hg38 | 56553 | hg19 | 56553 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv13606242, essv13606243, essv13606251, essv13606241, essv13606244, essv13606252, essv13606240, essv13606249, essv13606250, essv13606245, essv13606248, essv13606247, essv13606246 | Samples | HG01882, NA19209, HG03189, NA18865, NA19210, HG03169, NA20126, HG02541, HG02337, HG03297, NA19391, NA18867, NA19204 | Known Genes | INIP, KIAA1958 | Method | Sequencing | Analysis | | Platform | Multiple platforms | Comments | | Reference | 1000_Genomes_Consortium_Phase_3 | Pubmed ID | 21293372 | Accession Number(s) | esv3621518
| Frequency | Sample Size | 2504 | Observed Gain | 13 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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