Variant DetailsVariant: esv2714948| Internal ID | 10298584 | | 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 |
|
|