Variant DetailsVariant: esv2670934 Internal ID | 9590353 | Landmark | | Location Information | | Cytoband | 17q12 | Allele length | Assembly | Allele length | hg38 | 28401 | hg19 | 28436 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6285967, essv6434203, essv5841977, essv6437415, essv6538630, essv5444840, essv6372989, essv6005266, essv5524390, essv6169229, essv6536948, essv5701619, essv5469687, essv5413485, essv6423332, essv5769730, essv5836396, essv6231608, essv6591452, essv6148431, essv6345212, essv5929130, essv6324403 | Samples | NA18861, NA12751, NA18870, NA18510, NA18489, NA18558, NA19238, NA12044, NA19239, NA18956, NA18871, NA18566, NA19114, NA18499, NA18853, NA19257, NA18523, NA18858, NA18608, NA18542, NA19147, NA19240, NA19102 | Known Genes | CCL3, CCL4 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2670934
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
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