Variant DetailsVariant: esv2714948| Internal ID | 9949233 |  | Landmark |  |  | Location Information |  |  | Cytoband | 16q24.2 |  | Allele length | | Assembly | Allele length |  | hg38 | 281 |  | hg19 | 281 |  
  |  | Variant Type | CNV deletion |  | Copy Number |  |  | Allele State |  |  | Allele Origin |  |  | Probe Count |  |  | Validation Flag |  |  | Merged Status | M |  | Merged Variants |  |  | Supporting Variants | essv6763748, essv6815972, essv6874099, essv6831890, essv6920828, essv6768959, essv6714543, essv6766104, essv6744416 |  | Samples | SSM064, SSM062, SSM017, SSM006, SSM081, SSM053, SSM077, SSM091, SSM063 |  | Known Genes | BANP |  | Method | Sequencing |  | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads |  | Platform | Illumina HiSeq 2000 |  | Comments |  |  | Reference | Wong_et_al_2012b |  | Pubmed ID | 23290073 |  | Accession Number(s) | esv2714948
  |  | Frequency | | Sample Size | 96 |  | Observed Gain | 0 |  | Observed Loss | 9 |  | Observed Complex | 0 |  | Frequency | n/a |  
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