Variant DetailsVariant: esv2715164 Internal ID | 9949450 | Landmark | | Location Information | | Cytoband | 16q24.3 | Allele length | Assembly | Allele length | hg38 | 242 | hg19 | 242 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6895196, essv6932538, essv6713548, essv6916714, essv6971479, essv6784224, essv6800894, essv6732762, essv6796672, essv6780058, essv6835466, essv6941004, essv6843089, essv6776288, essv6721301, essv6953900, essv6725104, essv6936843, essv6706755, essv6913222 | Samples | SSM071, SSM045, SSM042, SSM028, SSM084, SSM021, SSM047, SSM067, SSM044, SSM066, SSM068, SSM040, SSM072, SSM082, SSM020, SSM015, SSM016, SSM022, SSM025, SSM098 | 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) | esv2715164
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 20 | Observed Complex | 0 | Frequency | n/a |
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