| Variant DetailsVariant: essv6944512| Internal ID | 9706433 |  | Landmark |  |  | Location Information |  |  | Cytoband | 10p15.2 |  | Allele length | | Assembly | Allele length |  | hg38 | 359 |  | hg19 | 359 | 
 |  | Variant Type | CNV deletion |  | Copy Number |  |  | Allele State |  |  | Allele Origin |  |  | Probe Count |  |  | Validation Flag |  |  | Merged Status | S |  | Merged Variants | esv2731484, esv2730995 |  | Supporting Variants |  |  | Samples | SSM023 |  | Known Genes |  |  | 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) | essv6944512 
 |  | Frequency | | Sample Size | 96 |  | Observed Gain | 0 |  | Observed Loss | 1 |  | Observed Complex | 0 |  | Frequency | n/a | 
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