Variant DetailsVariant: esv2749882Internal ID | 9984166 | Landmark | | Location Information | | Cytoband | 15q24.1 | Allele length | Assembly | Allele length | hg38 | 265 | hg19 | 265 |
| Variant Type | CNV deletion | Copy Number | | Allele State | | Allele Origin | | Probe Count | | Validation Flag | | Merged Status | M | Merged Variants | dgv307e201 | Supporting Variants | essv6879791, essv6788193, essv6776092, essv6809717, essv6724892, essv6706585, essv6909297, essv6857888, essv6673862, essv6901720, essv6862916, essv6755895, essv6772497, essv6942496, essv6665346, essv6869542, essv6867705, essv6842879, essv6851890, essv6800661, essv6678246, essv6871057, essv6732537 | Samples | SSM075, SSM045, SSM011, SSM065, SSM087, SSM093, SSM088, SSM058, SSM084, SSM090, SSM047, SSM069, SSM029, SSM089, SSM032, SSM003, SSM031, SSM014, SSM086, SSM066, SSM040, SSM072, SSM012 | Known Genes | CSK | 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) | esv2749882
| Frequency | Sample Size | 96 | Observed Gain | 0 | Observed Loss | 23 | Observed Complex | 0 | Frequency | n/a |
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