Variant DetailsVariant: esv3890644Internal ID | 18838042 | Landmark | | Location Information | | Cytoband | 5q13.2 | Allele length | Assembly | Allele length | hg38 | 107962 | hg19 | 107962 | hg18 | 107962 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25780619, essv25780808, essv25780623, essv25786184, essv25792626, essv25783860, essv25780815, essv25779683, essv25780546, essv25783942, essv25783971, essv25784390, essv25779665, essv25789178, essv25783393, essv25784600, essv25782594, essv25779846, essv25789197, essv25788748, essv25783885, essv25787038, essv25785088 | Samples | | Known Genes | GTF2H2, GTF2H2B, GTF2H2C, GTF2H2D, LOC647859, NAIP | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3890644
| Frequency | Sample Size | 3017 | Observed Gain | 4 | Observed Loss | 19 | Observed Complex | 0 | Frequency | n/a |
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