Variant DetailsVariant: esv2715161 Internal ID | 9949447 | Landmark | | Location Information | | Cytoband | 16q24.3 | Allele length | Assembly | Allele length | hg38 | 804 | hg19 | 804 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6953899, essv6732761, essv6852159, essv6696204, essv6916713, essv6674164, essv6792500, essv6941003, essv6839260, essv6682163, essv6728894, essv6668503, essv6721300, essv6888494, essv6812659, essv6706753, essv6920852, essv6796671, essv6780057, essv6932537, essv6725103, essv6713547, essv6710001, essv6936842, essv6800893, essv6913221, essv6971478, essv6665675, essv6678442 | Samples | SSM022, SSM086, SSM033, SSM042, SSM040, SSM031, SSM025, SSM072, SSM020, SSM071, SSM016, SSM032, SSM045, SSM067, SSM083, SSM041, SSM017, SSM028, SSM029, SSM030, SSM047, SSM021, SSM037, SSM046, SSM096, SSM044, SSM015, SSM076, 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) | esv2715161
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 29 | Observed Complex | 0 | Frequency | n/a |
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