Variant DetailsVariant: esv2718930 Internal ID | 9953222 | Landmark | | Location Information | | Cytoband | 19q13.42 | Allele length | Assembly | Allele length | hg38 | 17906 | hg19 | 17906 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6738672, essv6937390, essv6780570, essv6880268, essv6933033, essv6758906, essv6717543, essv6828778, essv6846781, essv6717913, essv6782377, essv6668767, essv6898432, essv6874507, essv6804251, essv6883105, essv6721749, essv6961086, essv6717587, essv6744780, essv6925428, essv6750436, essv6863680, essv6666558 | Samples | SSM059, SSM008, SSM073, SSM093, SSM050, SSM088, SSM021, SSM018, SSM029, SSM026, SSM094, SSM067, SSM044, SSM006, SSM085, SSM020, SSM053, SSM080, SSM091, SSM099, SSM043, SSM056, SSM030 | Known Genes | KIR2DL4, KIR3DL1, LOC100287534 | Method | Sequencing | Analysis | Breakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads | Platform | Illumina HiSeq 2000 | Comments | | Reference | Wong_et_al_2012b | Pubmed ID | 23290073 | Accession Number(s) | esv2718930
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
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