Variant DetailsVariant: esv3892007 Internal ID | 18839717 | Landmark | | Location Information | | Cytoband | 11q11 | Allele length | Assembly | Allele length | hg38 | 59812 | hg19 | 59812 | hg18 | 59812 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25780137, essv25800683, essv25797640, essv25785314, essv25781078, essv25781282, essv25784933, essv25785370, essv25782359, essv25780072, essv25784559, essv25781455, essv25781541, essv25798378, essv25781254, essv25782349, essv25782330, essv25786837, essv25784227, essv25782250, essv25800594, essv25799866, essv25781998, essv25783738, essv25782600, essv25800322, essv25800311, essv25784497, essv25778520, essv25781962, essv25786559, essv25787008, essv25779495, essv25780845, essv25785345, essv25796929, essv25800141, essv25786396, essv25785149, essv25782818, essv25782160, essv25780320, essv25780246, essv25783309, essv25799918, essv25782012, essv25782279, essv25782194, essv25783175, essv25780220, essv25799828, essv25780797, essv25780144, essv25800744, essv25784282, essv25783131, essv25783522, essv25783531 | Samples | | Known Genes | OR4C11, OR4P4, OR4S2 | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 Illumina Human OmniExpress | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3892007
| Frequency | Sample Size | 3017 | Observed Gain | 0 | Observed Loss | 58 | Observed Complex | 0 | Frequency | n/a |
|
|