Variant DetailsVariant: esv3293718| Internal ID | 10966698 |  | Landmark |  |  | Location Information |  |  | Cytoband | 5p12 |  | Allele length | | Assembly | Allele length |  | hg38 | 578 |  | hg19 | 578 |  
  |  | Variant Type | CNV deletion |  | Copy Number |  |  | Allele State |  |  | Allele Origin |  |  | Probe Count |  |  | Validation Flag |  |  | Merged Status | M |  | Merged Variants |  |  | Supporting Variants | essv7563285 |  | Samples | HuRef |  | Known Genes |  |  | Method | Sequencing |  | Analysis |  |  | Platform | Complete Genomics |  | Comments |  |  | Reference | Pang_et_al_2013b |  | Pubmed ID | 24192839 |  | Accession Number(s) | esv3293718
  |  | Frequency | | Sample Size | 1 |  | Observed Gain | 0 |  | Observed Loss | 1 |  | Observed Complex | 0 |  | Frequency | n/a |  
  |  
  |