Variant DetailsVariant: dgv4425n54Internal ID | 20137849 | Landmark | | Location Information | | Cytoband | 15q13.2 | Allele length | Assembly | Allele length | hg38 | 224103 | hg19 | 224103 | hg18 | 224103 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv568759, nsv568761, nsv568760, nsv568754, nsv568751, nsv568753, nsv568750 | Samples | HGDP01214 | Known Genes | ARHGAP11B, GOLGA8H, HERC2P10, LOC100288637 | 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) | dgv4425n54
| Frequency | Sample Size | 17421 | Observed Gain | 8 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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