Variant DetailsVariant: esv2732746| Internal ID | 9967067 | | Landmark | | | Location Information | | | Cytoband | 6q23.3 | | Allele length | | Assembly | Allele length | | hg38 | 223 | | hg19 | 223 |
| | Variant Type | CNV deletion | | Copy Number | | | Allele State | | | Allele Origin | | | Probe Count | | | Validation Flag | | | Merged Status | M | | Merged Variants | | | Supporting Variants | essv6855987, essv6957167, essv6719539, essv6860982, essv6907686, essv6855369, essv6878692, essv6963881, essv6849279, essv6671249 | | Samples | SSM027, SSM011, SSM087, SSM093, SSM088, SSM026, SSM031, SSM044, SSM014, SSM086 | | 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) | esv2732746
| | Frequency | | Sample Size | 96 | | Observed Gain | 0 | | Observed Loss | 10 | | Observed Complex | 0 | | Frequency | n/a |
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