Variant DetailsVariant: esv2745287 Internal ID | 9979571 | Landmark | | Location Information | | Cytoband | 11q25 | Allele length | Assembly | Allele length | hg38 | 293 | hg19 | 293 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6702397, essv6783518, essv6965696, essv6815422, essv6806337, essv6673080, essv6867084, essv6882282, essv6959177, essv6887971, essv6728279, essv6927877, essv6724447, essv6916069, essv6931778, essv6894600, essv6900604, essv6857122, essv6891237, essv6823577, essv6709441, essv6819640, essv6851090, essv6879441, essv6970745, essv6831260, essv6677761 | Samples | SSM100, SSM027, SSM045, SSM046, SSM079, SSM087, SSM097, SSM039, SSM093, SSM074, SSM041, SSM028, SSM096, SSM026, SSM089, SSM019, SSM094, SSM032, SSM031, SSM086, SSM068, SSM081, SSM020, SSM078, SSM016, SSM077, SSM098 | Known Genes | OPCML | 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) | esv2745287
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 27 | Observed Complex | 0 | Frequency | n/a |
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