Variant DetailsVariant: dgv5764n54Internal ID | 20139188 | Landmark | | Location Information | | Cytoband | 17q24.3 | Allele length | Assembly | Allele length | hg38 | 3589 | hg19 | 3589 | hg18 | 3589 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | nsv575969, nsv575976, nsv575964, nsv575968, nsv575970, nsv575965 | Samples | | Known Genes | SLC39A11 | 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) | dgv5764n54
| Frequency | Sample Size | 17421 | Observed Gain | 0 | Observed Loss | 17 | Observed Complex | 0 | Frequency | n/a |
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