Variant DetailsVariant: esv2745746Internal ID | 9980030 | Landmark | | Location Information | | Cytoband | 12p11.21 | Allele length | Assembly | Allele length | hg38 | 524 | hg19 | 524 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv185e201 | Supporting Variants | essv6737894, essv6851185, essv6741074, essv6867167, essv6765769, essv6772055, essv6819698, essv6687489, essv6862388 | Samples | SSM065, SSM050, SSM088, SSM089, SSM086, SSM078, SSM005, SSM052, SSM063 | Known Genes | BICD1 | 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) | esv2745746
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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