Variant DetailsVariant: esv2714948Internal 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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