Variant DetailsVariant: esv3893299Internal ID | 18837433 | Landmark | | Location Information | | Cytoband | 20p12.1 | Allele length | Assembly | Allele length | hg38 | 256676 | hg19 | 256676 | hg18 | 256676 |
| Variant Type | CNV loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25798056, essv25799084, essv25797045, essv25780832, essv25796374, essv25782484, essv25778349 | Samples | | Known Genes | MACROD2, MACROD2-AS1 | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 Illumina Human OmniExpress | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3893299
| Frequency | Sample Size | 3017 | Observed Gain | 0 | Observed Loss | 7 | Observed Complex | 0 | Frequency | n/a |
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