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Table 1 Summary of CNAs detected by aCGH

From: An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case

Chr.

Start –End band

Genomic position: start- end GRCh37/hg19

Variant type

Size (Mb)

COSMIC census cancer gene(s) within the region

7

p22.3p15.2

109,626-26,260,755

loss

26.1

CARD11, PMS2, RAC1, MACC1, HNRNPA2B1

p14.2p11.2

35,292,065-56,174,888

loss

20.8

SFRP4, IKZF1, EGFR

8

p23.3p11.1

176,452-43,399,198

gain

43.2

ARHGEF10, PCM1, LEPROTL1, WRN, NRG1, NSD3, FGFR1, ANK1, KAT6A, IKBKB, HOOK3

q11.1q24.3

46,939,154-146,294,098

gain

99.3

TCEA1, PLAG1, CHCHD7, PREX2, NCOA2, HEY1, CNBD1, NBN, RUNX1T1, CDH17, COX6C, PABPC1, UBR5, EIF3E, RSPO2, CSMD3, RAD21, EXT1, MYC, NDRG1, FAM135B, RECQL4

9

p24.3p13.2

207,437-37,270,400

loss

37.1

JAK2, CD274, PDCD1LG2, PTPRD, NFIB, PSIP1, MLLT3, CDKN2A, FANCG, PAX5

13

q12.3q24

32,035,219-115,059,020

loss

83.0

BRCA2, NBEA, LHFPL6, FOXO1, LCP1, RB1, CYSLTR2, GPC5, SOX21, ERCC5,

20

p13p11.1

60,747-25,713,574

gain

25.6

SIRPA, CRNKL1,

q11.2

29,467,937-29,948,374

gain

0.5

n.a.

q13.13

46,828,431-48,880,347

gain

2.05

n.a.