Variant DetailsVariant: dgv262e55Internal ID | 20126741 | Landmark | | Location Information | | Cytoband | 9q32 | Allele length | Assembly | Allele length | hg38 | 220949 | hg19 | 220949 | hg18 | 220949 | hg17 | 220949 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv34346, esv35051, esv34763, esv34739 | Samples | NA19204, NA19209, NA19210, NA19211 | Known Genes | INIP, KIAA1958, SNX30 | Method | SNP array | Analysis | | Platform | Affymetrix Mapping 250K Nsp SNP Array Affymetrix Mapping 250K Sty2 SNP Array | Comments | | Reference | Pinto_et_al_2007 | Pubmed ID | 17911159 | Accession Number(s) | dgv262e55
| Frequency | Sample Size | 771 | Observed Gain | 17 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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