Variant DetailsVariant: essv5161492Internal ID | 7906206 | Landmark | | Location Information | | Cytoband | 19q13.2 | Allele length | Assembly | Allele length | hg38 | 610060 | hg19 | 610060 | hg18 | 610060 | hg17 | 610060 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | S | Merged Variants | esv2422227 | Supporting Variants | | Samples | ND01548 | Known Genes | CEACAM8, LIPE-AS1, LOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG3, PSG6, PSG7, PSG8 | 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) | essv5161492
| Frequency | Sample Size | 181 | Observed Gain | 0 | Observed Loss | 1 | Observed Complex | 0 | Frequency | n/a |
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