Variant DetailsVariant: esv3893000Internal ID | 18837134 | Landmark | | Location Information | | Cytoband | 17q12 | Allele length | Assembly | Allele length | hg38 | 86448 | hg19 | 86449 | hg18 | 86449 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25792899, essv25788433, essv25788181, essv25788077, essv25788666, essv25788028, essv25787942, essv25785011, essv25787829, essv25789748, essv25791006, essv25788004, essv25785986, essv25789306, essv25789054, essv25788072, essv25788994, essv25788197, essv25782315, essv25789017 | Samples | | Known Genes | CCL3, CCL4, TBC1D3B | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 Illumina Human OmniExpress | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3893000
| Frequency | Sample Size | 3017 | Observed Gain | 17 | Observed Loss | 3 | Observed Complex | 0 | Frequency | n/a |
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