| Variant DetailsVariant: esv2724158| Internal ID | 9958459 |  | Landmark |  |  | Location Information |  |  | Cytoband | 22q12.3 |  | Allele length | | Assembly | Allele length |  | hg38 | 130 |  | hg19 | 130 | 
 |  | Variant Type | CNV deletion |  | Copy Number |  |  | Allele State |  |  | Allele Origin |  |  | Probe Count |  |  | Validation Flag |  |  | Merged Status | M |  | Merged Variants |  |  | Supporting Variants | essv6858917, essv6961181, essv6967628, essv6674948, essv6863745, essv6852940 |  | Samples | SSM027, SSM087, SSM088, SSM026, SSM031, SSM086 |  | Known Genes | LARGE |  | 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) | esv2724158 
 |  | Frequency | | Sample Size | 96 |  | Observed Gain | 0 |  | Observed Loss | 6 |  | Observed Complex | 0 |  | Frequency | n/a | 
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