Variant DetailsVariant: esv2729573 Internal ID | 9963888 | Landmark | | Location Information | | Cytoband | 10p15.3 | Allele length | Assembly | Allele length | hg38 | 716 | hg19 | 716 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6749399, essv6783151, essv6873410, essv6923924, essv6795645, essv6809094, essv6716393, essv6935918, essv6740741, essv6720329, essv6895776, essv6775362, essv6684821, essv6779090, essv6806094, essv6799832, essv6897363, essv6830955, essv6927606, essv6787367, essv6771699, essv6904561, essv6948670, essv6768509, essv6845657, essv6968296, essv6838273, essv6862686, essv6958614 | Samples | SSM008, SSM083, SSM071, SSM024, SSM075, SSM011, SSM065, SSM013, SSM074, SSM018, SSM069, SSM026, SSM019, SSM003, SSM067, SSM044, SSM066, SSM085, SSM068, SSM081, SSM072, SSM005, SSM091, SSM004, SSM099, SSM043, SSM052, SSM056, SSM012 | 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) | esv2729573
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 29 | Observed Complex | 0 | Frequency | n/a |
|
|