Variant DetailsVariant: esv2714946Internal ID | 9949231 | Landmark | | Location Information | | Cytoband | 16q24.2 | Allele length | Assembly | Allele length | hg38 | 323 | hg19 | 323 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6784212, essv6924922, essv6839243, essv6674145, essv6945627, essv6696188, essv6815971, essv6920827, essv6772676, essv6721286 | Samples | SSM083, SSM065, SSM023, SSM018, SSM017, SSM031, SSM044, SSM068, SSM037, SSM077 | 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) | esv2714946
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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