Variant DetailsVariant: dgv5660n54Internal ID | 20139084 | Landmark | | Location Information | | Cytoband | 17q21.31 | Allele length | Assembly | Allele length | hg38 | 125205 | hg19 | 125205 | hg18 | 125071 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv575400, nsv575398, nsv575404, nsv575406, nsv575402, nsv575409, nsv575401 | Samples | | Known Genes | ARL17A, ARL17B, NSF, NSFP1 | 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) | dgv5660n54
| Frequency | Sample Size | 17421 | Observed Gain | 22 | Observed Loss | 52 | Observed Complex | 0 | Frequency | n/a |
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