Variant DetailsVariant: dgv5535n54| Internal ID | 22773430 | | Landmark | | | Location Information | | | Cytoband | 17q12 | | Allele length | | Assembly | Allele length | | hg38 | 49898 | | hg19 | 49885 | | hg18 | 49885 |
| | Variant Type | CNV gain | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | nsv574765, nsv574761, nsv574758, nsv574766, nsv574764 | | Samples | | | Known Genes | CCL4 | | 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) | dgv5535n54
| | Frequency | | Sample Size | 17421 | | Observed Gain | 28 | | Observed Loss | 0 | | Observed Complex | 0 | | Frequency | n/a |
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