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. Author manuscript; available in PMC: 2018 Apr 10.
Published in final edited form as: Exp Hematol. 2009 May 27;37(8):937–946. doi: 10.1016/j.exphem.2009.04.012

Figure 6. Homozygous deletion of 19p13.3 by acquired uniparental disomy in MCL.

Figure 6

Top panel: aUPD was found on 19p leading to homozygous deletion of 19p13.1 in MCL case #21699. Middle panel: SNP-chip probe signals on 19p. Bottom panel: Eight genes involved in homozygous deletion caused by aUPD. TNF superfamily genes (TNFSF 7, 9, 14) are homozygously deleted in this case. Arrows indicate the directions and approximate relative sizes of the genes located in this region.