Variant DetailsVariant: dgv1109n54 Internal ID | 20134533 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 166502 | hg19 | 166502 | hg18 | 166502 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv550765, nsv550748, nsv550752, nsv550749, nsv550754, nsv550753, nsv550756, nsv550767, nsv550766, nsv550733, nsv550734, nsv550750 | Samples | HGDP00157, HGDP01379, 1780862307_A, HGDP00127, HGDP00884, HGDP00646, HGDP00654, HGDP00888, HGDP00136, HGDP00428, HGDP00021, 1782681313_A, 1798860592_A, HGDP00787, HGDP00785, HGDP01296, 1780862360_A, HGDP00208, HGDP01352, 1782681296_A, HGDP00143, HGDP00658, HGDP00134, HGDP00364, 1798860569_A, HGDP00681, HGDP01177, 1780854296_A, 1787431196_A | Known Genes | ANTXRL, ANTXRLP1 | 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) | dgv1109n54
| Frequency | Sample Size | 17421 | Observed Gain | 58 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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