Variant DetailsVariant: esv3891136Internal ID | 18838846 | Landmark | | Location Information | | Cytoband | 7q11.21 | Allele length | Assembly | Allele length | hg38 | 591221 | hg19 | 591221 | hg18 | 591221 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25788083 | Samples | | Known Genes | GTF2IRD1P1, LOC101929736, MIR4650-1, MIR4650-2, PMS2P4, RABGEF1, SBDS, STAG3L4, TMEM248, TYW1 | Method | SNP array | Analysis | | Platform | Illumina Human OmniExpress | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3891136
| Frequency | Sample Size | 3017 | Observed Gain | 1 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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