Variant DetailsVariant: nsv556947 Internal ID | 15997670 | Landmark | | Location Information | | Cytoband | 12p13.33 | Allele length | Assembly | Allele length | hg38 | 653 | hg19 | 653 | hg18 | 653 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv2261n54 | Supporting Variants | nssv786258, nssv786235, nssv786270, nssv786278, nssv786262, nssv786263, nssv786241, nssv786250, nssv786265, nssv786264, nssv786238, nssv786260, nssv786257, nssv786237, nssv786274, nssv786273, nssv786248, nssv786255, nssv786253, nssv786269, nssv786252, nssv786240, nssv786261, nssv786279, nssv786239, nssv786243, nssv786268, nssv786277, nssv786244, nssv786276, nssv786249, nssv786267, nssv786272, nssv786247, nssv786266, nssv786256, nssv786242, nssv786275, nssv786236, nssv786259, nssv786254, nssv786245, nssv786271, nssv786246, nssv786251 | Samples | | Known Genes | ERC1 | 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) | nsv556947
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 45 | Observed Complex | 0 | Frequency | n/a |
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