Variant DetailsVariant: esv3892664Internal ID | 18836798 | Landmark | | Location Information | | Cytoband | 15q14 | Allele length | Assembly | Allele length | hg38 | 166792 | hg19 | 166792 | hg18 | 166792 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25798129, essv25793022, essv25782823, essv25782763, essv25788758, essv25782956, essv25787443, essv25799182, essv25788886, essv25788972, essv25798120, essv25793119, essv25790735, essv25799778, essv25788883, essv25790261, essv25800581, essv25785670, essv25789482, essv25798997, essv25779589 | Samples | | Known Genes | GOLGA8A, GOLGA8B, MIR1233-1, MIR1233-2 | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3892664
| Frequency | Sample Size | 3017 | Observed Gain | 9 | Observed Loss | 12 | Observed Complex | 0 | Frequency | n/a |
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