Variant DetailsVariant: esv3892998Internal ID | 18837132 | Landmark | | Location Information | | Cytoband | 17q12 | Allele length | Assembly | Allele length | hg38 | 189288 | hg19 | 189288 | hg18 | 189288 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25800819 | Samples | | Known Genes | FNDC8, NLE1, RAD51D, RAD51L3-RFFL, SLC35G3, SLFN5, UNC45B | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3892998
| Frequency | Sample Size | 3017 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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