Variant DetailsVariant: dgv3146n100Internal ID | 20154762 | Landmark | | Location Information | | Cytoband | 17q12 | Allele length | Assembly | Allele length | hg38 | 109387 | hg19 | 109395 | hg18 | 109395 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv1055883, nsv1066491, nsv1062221, nsv1055919, nsv1066525, nsv1065718, nsv1064821, nsv1060483, nsv1059803, nsv1055256, nsv1066064, nsv1059751, nsv1056044, nsv1066816, nsv1066773, nsv1056130 | Samples | | Known Genes | CCL3L1, CCL3L3, CCL4, TBC1D3B | Method | SNP array | Analysis | Affymetrix SNP array copy number analysis | Platform | Affymetrix SNP Array 6.0 | Comments | | Reference | Coe_et_al_2014 | Pubmed ID | 25217958 | Accession Number(s) | dgv3146n100
| Frequency | Sample Size | 29084 | Observed Gain | 215 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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