Variant DetailsVariant: esv3891678Internal ID | 18839388 | Landmark | | Location Information | | Cytoband | 9q21.11 | Allele length | Assembly | Allele length | hg38 | 226176 | hg19 | 226176 | hg18 | 226176 |
| Variant Type | CNV gain | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25788842, essv25788959, essv25788860, essv25788993 | Samples | | Known Genes | FXN, PIP5K1B, PRKACG, TJP2 | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3891678
| Frequency | Sample Size | 3017 | Observed Gain | 4 | Observed Loss | 0 | Observed Complex | 0 | Frequency | n/a |
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