Table 3.

Most frequently lost clones in MCL


Clone name

Base position, Kb

Cytogenetic band

% of cases with copy number loss

Genes in affected interval
Group A     
RP11-89b24   Chr1:94,003   1p22.1   77  PARG1, TGFBR3, GF11 
RP11-122a8   Chr13:98,597   13q32.3   67  ZIZIMIN1, STK24, EBI2 
RP11-246o4   Chr1:82,559   1p31.1   62   —  
RP11-19j14   Chr13:97,890   13q32.2   62  FARP1, STK24, DOCK9 
RP11-65f22   Chr22:31,034   22q12.3   62  SLC5A4, LIF, PES1 
RP11-40h10   Chr13:94,399   13q32.1   57   —  
RP11-17i11   Chr13:42,711   13q14.11   57  DNAJD1, MJC 
Group B     
RP11-58f7*  Chr7:156,972   7q36.3   79  PTPRN2 
RP11-3p8   Chr13:111,893   13q34   75  ING1, SOX1 
RP11-88j24   Chr1:36,922   1p34.3   73  GRIK3 
CTC-200d12*  Chr14:104,922   14q32.33   71  IGHM 
RP11-19o15   Chr13:112,427   13q34   69  TUBGCP3 
RP11-58c16   Chr13:50,175   13q14.3   67  NEK3, CKAP2 
RP11-278e23   Chr22:17,193   22q11.21   64  DRCR6, ZNF74, HIC2 
RP11-2111   Chr1:14,410   1p36.21   57  MGC4342 
RP11-2c23   Chr11:20,127   11p15.1   57  NAV2 
RP11-79d15   Chr1:17,016   1p36.13   57  PAD12 SDHN, PAX7 
Group C     
RP11-55m23  Chr1:54,836   1p32.3   77  BSND 
RP11-116m19   Chr2:236,646   2q37.2   62  CENTG2, SH3BP4 
RP4-771p4   Chr7:73,000   7q11.23   62  LIMK, RFC21 
RP11-14k9
 
Chr5:168,448
 
5q35.1
 
62
 
SLIT3, RARS, PANK3
 

Clone name

Base position, Kb

Cytogenetic band

% of cases with copy number loss

Genes in affected interval
Group A     
RP11-89b24   Chr1:94,003   1p22.1   77  PARG1, TGFBR3, GF11 
RP11-122a8   Chr13:98,597   13q32.3   67  ZIZIMIN1, STK24, EBI2 
RP11-246o4   Chr1:82,559   1p31.1   62   —  
RP11-19j14   Chr13:97,890   13q32.2   62  FARP1, STK24, DOCK9 
RP11-65f22   Chr22:31,034   22q12.3   62  SLC5A4, LIF, PES1 
RP11-40h10   Chr13:94,399   13q32.1   57   —  
RP11-17i11   Chr13:42,711   13q14.11   57  DNAJD1, MJC 
Group B     
RP11-58f7*  Chr7:156,972   7q36.3   79  PTPRN2 
RP11-3p8   Chr13:111,893   13q34   75  ING1, SOX1 
RP11-88j24   Chr1:36,922   1p34.3   73  GRIK3 
CTC-200d12*  Chr14:104,922   14q32.33   71  IGHM 
RP11-19o15   Chr13:112,427   13q34   69  TUBGCP3 
RP11-58c16   Chr13:50,175   13q14.3   67  NEK3, CKAP2 
RP11-278e23   Chr22:17,193   22q11.21   64  DRCR6, ZNF74, HIC2 
RP11-2111   Chr1:14,410   1p36.21   57  MGC4342 
RP11-2c23   Chr11:20,127   11p15.1   57  NAV2 
RP11-79d15   Chr1:17,016   1p36.13   57  PAD12 SDHN, PAX7 
Group C     
RP11-55m23  Chr1:54,836   1p32.3   77  BSND 
RP11-116m19   Chr2:236,646   2q37.2   62  CENTG2, SH3BP4 
RP4-771p4   Chr7:73,000   7q11.23   62  LIMK, RFC21 
RP11-14k9
 
Chr5:168,448
 
5q35.1
 
62
 
SLIT3, RARS, PANK3
 

In group A, hotspots are present in the smallest regions of overlap. In group B, hotspots are present in consecutive areas. In group C, hotspots are not present in any of the consecutive areas. Mb positions of the clones were determined with USSC genome browser (April 2003 freeze). Hotspots were defined as clones with a ratio < −0.3 in 8 or more of the 14 cases. Percentages were calculated by dividing the number of cases with ratio < −0.3 with the number of samples that gave a hydridization signal. RP11-19j14 and RP11-122a8, RP11-3p8 and RP11-19o15 are consecutive clones.

— indicates that there are no known genes in the interval.

*

These clones were identified as polymorphisms in the human genome by either Sebat et al27  or lafrate et al.28 

This clone was mapped to different locations using the USSC genome browser; in this table the position in FISH clone track was used for this table. Genes were identified in the Mb region between the flanking clones of a hotspot.

Close Modal

or Create an Account

Close Modal
Close Modal