Variant DetailsVariant: dgv535e201Internal ID | 20125422 | Landmark | | Location Information | | Cytoband | 19q13.42 | Allele length | Assembly | Allele length | hg38 | 23714 | hg19 | 23699 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | esv2718912, esv2718919 | Samples | SSM008, SSM011, SSM042, SSM023, SSM092, SSM021, SSM018, SSM029, SSM003, SSM085, SSM081, SSM082, SSM020, SSM015, SSM078, SSM080, SSM010, SSM070, SSM098 | Known Genes | KIR2DL3, KIR3DL3 | 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) | dgv535e201
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 19 | Observed Complex | 0 | Frequency | n/a |
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