Variant DetailsVariant: esv3892303Internal ID | 18836437 | Landmark | | Location Information | | Cytoband | 1p36.13 | Allele length | Assembly | Allele length | hg38 | 99311 | hg19 | 99311 | hg18 | 99311 |
| Variant Type | CNV gain+loss | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv25786037, essv25784995, essv25798913, essv25786129, essv25800967, essv25791145, essv25785742 | Samples | | Known Genes | CROCC, MIR3675 | Method | SNP array | Analysis | | Platform | Illumina HumanHap 610 | Comments | | Reference | Suktitipat_et_al_2014 | Pubmed ID | 25118596 | Accession Number(s) | esv3892303
| Frequency | Sample Size | 3017 | Observed Gain | 1 | Observed Loss | 6 | Observed Complex | 0 | Frequency | n/a |
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