Variant DetailsVariant: esv2729585 Internal ID | 9963900 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 887 | hg19 | 887 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6827321, essv6727967, essv6904563, essv6919768, essv6802854, essv6731740, essv6832177, essv6834564, essv6795646, essv6931430, essv6712675, essv6716394, essv6771700, essv6882049, essv6970383, essv6768520, essv6952831, essv6850574, essv6876381, essv6743751, essv6944492, essv6830956, essv6684766, essv6976426, essv6768215, essv6842080 | Samples | SSM008, SSM071, SSM046, SSM064, SSM065, SSM013, SSM009, SSM042, SSM023, SSM028, SSM092, SSM084, SSM047, SSM029, SSM017, SSM094, SSM086, SSM081, SSM082, SSM020, SSM053, SSM080, SSM010, SSM025, SSM034, SSM043 | Known Genes | ADARB2 | 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) | esv2729585
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 26 | Observed Complex | 0 | Frequency | n/a |
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