Variant DetailsVariant: esv3891801Internal ID | 18839511 | Landmark | | Location Information | | Cytoband | 10q11.22 | Allele length | Assembly | Allele length | hg38 | 204534 | hg19 | 204515 | hg18 | 204515 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25788097, essv25801067, essv25787766, essv25779970, essv25792688, essv25787976, essv25782234, essv25788756, essv25781611, essv25789122, essv25798027, essv25781556, essv25788489, essv25789020, essv25787786, essv25788828, essv25798736, essv25788213, essv25789382, essv25792249, essv25796822, essv25798574, essv25792540, essv25789513 | Samples | | Known Genes | ANTXRL, ANTXRLP1, FAM25B | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 Illumina Human OmniExpress | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3891801
| Frequency | Sample Size | 3017 | Observed Gain | 15 | Observed Loss | 9 | Observed Complex | 0 | Frequency | n/a |
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