Variant DetailsVariant: esv3891440Internal ID | 18839150 | Landmark | | Location Information | | Cytoband | 8q21.3 | Allele length | Assembly | Allele length | hg38 | 60451 | hg19 | 60451 | hg18 | 60451 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25784457, essv25787222, essv25799784, essv25779450, essv25783973, essv25781830, essv25784314, essv25785041, essv25786963, essv25782611, essv25779168, essv25779494, essv25799431 | Samples | | Known Genes | LRRC69 | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3891440
| Frequency | Sample Size | 3017 | Observed Gain | 0 | Observed Loss | 13 | Observed Complex | 0 | Frequency | n/a |
|
|