Skip to main content

Table 1 Results of aCGH. Summary of CNAs detected by aCGH

From: A new childhood ALL case with an extremely complex karyotype and acute spontaneous tumor lysis syndrome

Chr.

Start–end band

Genomic position: start–end

GRCh37/hg19

Variant type

Size (Mb)

COSMIC census cancer gene(s) within the region

7

p22.3p22.1

45,130–4,642,192

1 copy gain

4.6

CARD11

7

q21.3q36.3

96,556,335–159,128,556

1 copy gain

62.6

TRRAP, CUX1, CREB3L2, MET, POT1, SND1, SMO, TRB, TRIM24, KIAA1549, BRAF, FAM131B, CNTNAP2, EZH2, KMT2C, MNX1

11

q24.2q25

125,246,792–134,945,165

1 copy loss

9.7

FLI1, KCNJ5

18

p11.22p11.21

9,095,620–14,089,409

1 copy gain

4.99

 

18

q11.1q23

18.550.472–78.012.829

1 copy gain

59.5

ZNF521,SS18, SETBP1, SMAD2, SMAD4, DCC, MALT1, BCL2, KDSR,