Variant DetailsVariant: esv2724157Internal ID | 9958458 | Landmark | | Location Information | | Cytoband | 22q12.3 | Allele length | Assembly | Allele length | hg38 | 780 | hg19 | 780 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6758937, essv6858917, essv6961181, essv6967628, essv6674948, essv6863745, essv6741995, essv6852940, essv6747653 | Samples | SSM059, SSM027, SSM087, SSM088, SSM026, SSM031, SSM086, SSM055, SSM052 | 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) | esv2724157
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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