Variant DetailsVariant: esv2660470 Internal ID | 9579889 | Landmark | | Location Information | | Cytoband | 17q12 | Allele length | Assembly | Allele length | hg38 | 44884 | hg19 | 44948 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv545e199 | Supporting Variants | essv5549904, essv6054715, essv5814807, essv5651689, essv6205307, essv6420687, essv6180739, essv6351134, essv5669936, essv6063646, essv6406012, essv6268492, essv6189114, essv6066863, essv5985494, essv6043484, essv6249881, essv6327283, essv5436959, essv6068875, essv5558459, essv6454682, essv5841836, essv5604524, essv6294372, essv6307910, essv6485280, essv6147112, essv6401447, essv5916398 | Samples | HG01441, HG01359, HG01389, HG01456, HG01461, HG01140, HG01350, HG01488, HG01354, HG01495, HG01440, HG01550, HG01124, HG01136, HG01384, HG01149, HG01390, HG01383, HG01497, HG01148, HG01253, HG01113, HG01489, HG01342, HG01491, HG01251, HG01378, HG01125, HG01112, HG01437 | Known Genes | CCL3L1, CCL3L3, CCL4L1, CCL4L2 | Method | Merging | Analysis | No reference, merging analysis | Platform | Merging | Comments | | Reference | 1000_Genomes_Consortium_Phase_1 | Pubmed ID | 23128226 | Accession Number(s) | esv2660470
| Frequency | Sample Size | 1151 | Observed Gain | 0 | Observed Loss | 30 | Observed Complex | 0 | Frequency | n/a |
|
|