Variant DetailsVariant: esv2660852Internal ID | 9580271 | Landmark | | Location Information | | Cytoband | 10q24.2 | Allele length | Assembly | Allele length | hg38 | 338 | hg19 | 338 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6244196, essv5929432, essv6180993, essv5940247, essv6346740, essv5448085, essv6509643, essv5989922, essv5819320, essv6276489 | Samples | NA19394, NA19397, NA18861, NA19819, NA19393, NA18510, NA19138, NA18907, NA18909, NA19129 | Known Genes | CRTAC1 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | High quality site | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2660852
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 10 | Observed Complex | 0 | Frequency | n/a |
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