Variant DetailsVariant: esv3892774Internal ID | 18836908 | Landmark | | Location Information | | Cytoband | 16p13.2 | Allele length | Assembly | Allele length | hg38 | 43296 | hg19 | 43296 | hg18 | 43296 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25783587, essv25779572, essv25798205, essv25798807 | Samples | | Known Genes | RBFOX1 | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3892774
| Frequency | Sample Size | 3017 | Observed Gain | 0 | Observed Loss | 4 | Observed Complex | 0 | Frequency | n/a |
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