Variant DetailsVariant: esv2732758 Internal ID | 9967079 | Landmark | | Location Information | | Cytoband | 6q23.3 | Allele length | Assembly | Allele length | hg38 | 995 | hg19 | 995 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv1016e201 | Supporting Variants | essv6790604, essv6903808, essv6704476, essv6887092, essv6802649, essv6872849, essv6881506, essv6869849, essv6719537, essv6929551, essv6923162, essv6676674, essv6930543, essv6814417, essv6723319, essv6782307, essv6947901, essv6794758, essv6798964, essv6727211, essv6855374, essv6705126, essv6865711, essv6899785, essv6830269, essv6849285, essv6671256, essv6918927 | Samples | SSM100, SSM071, SSM024, SSM045, SSM046, SSM087, SSM013, SSM073, SSM090, SSM018, SSM096, SSM089, SSM017, SSM094, SSM032, SSM003, SSM031, SSM044, SSM086, SSM006, SSM068, SSM081, SSM040, SSM072, SSM020, SSM077, SSM091, SSM070 | Known Genes | BCLAF1 | 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) | esv2732758
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 28 | Observed Complex | 0 | Frequency | n/a |
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