Variant DetailsVariant: essv5161300Internal ID | 7906014 | Landmark | | Location Information | | Cytoband | 12p13.31 | Allele length | Assembly | Allele length | hg38 | 295570 | hg19 | 295570 | hg18 | 295570 | hg17 | 295570 |
| Variant Type | CNV duplication | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2422373 | Supporting Variants | | Samples | ND05071 | Known Genes | APOBEC1, CLEC4C, DPPA3, GDF3, NANOG, NANOGNB, SLC2A14 | Method | SNP array | Analysis | log R ratio and B allele frequency. | Platform | Not specified | Comments | | Reference | Simon-Sanchez_et_al_2007 | Pubmed ID | 17116639 | Accession Number(s) | essv5161300
| Frequency | Sample Size | 181 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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