Variant DetailsVariant: nsv1066491Internal ID | 18809022 | Landmark | | Location Information | | Cytoband | 17q12 | Allele length | Assembly | Allele length | hg38 | 88141 | hg19 | 88148 | hg18 | 88148 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv3146n100 | Supporting Variants | nssv3561751, nssv3561756, nssv3561754, nssv3561752, nssv3561749, nssv3561753, nssv3561757, nssv3561750, nssv3561758, nssv3561755, nssv3720716 | Samples | | Known Genes | CCL3L1, CCL3L3, 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) | nsv1066491
| Frequency | Sample Size | 29084 | Observed Gain | 11 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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