Variant DetailsVariant: esv2715156Internal ID | 9949442 | Landmark | | Location Information | | Cytoband | 16q24.3 | Allele length | Assembly | Allele length | hg38 | 272 | hg19 | 272 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6966785, essv6706751, essv6820374, essv6824240, essv6916712, essv6691299, essv6792498, essv6888493, essv6895195, essv6800892 | Samples | SSM027, SSM040, SSM078, SSM072, SSM016, SSM005, SSM096, SSM079, SSM098, SSM070 | Known Genes | ANKRD11 | 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) | esv2715156
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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