Variant DetailsVariant: esv2737337Internal ID | 9971675 | Landmark | | Location Information | | Cytoband | 8q22.1 | Allele length | Assembly | Allele length | hg38 | 620 | hg19 | 620 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | | Supporting Variants | essv6705683, essv6814922, essv6672163, essv6976027, essv6879082, essv6755075, essv6881906, essv6873269, essv6775178, essv6760556, essv6749243, essv6740557, essv6958200, essv6964804, essv6935442, essv6850228 | Samples | SSM027, SSM093, SSM058, SSM021, SSM061, SSM029, SSM026, SSM094, SSM031, SSM086, SSM066, SSM040, SSM077, SSM091, SSM052, SSM056 | Known Genes | CPQ | 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) | esv2737337
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 16 | Observed Complex | 0 | Frequency | n/a |
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