Table 1 Clonality of somatic copy-number alterations identified in distinct neuroblastoma samples during the course of disease in 9 patients.

From: Spatial and temporal intratumour heterogeneity has potential consequences for single biopsy-based neuroblastoma treatment decisions

Patient

Risk group

# Clonal segments (% genome)

# Subclonal segments (% genome)

Biopsied samples

# Samples

MNA

CB1001

HR

100 (12%)

3 (0.4%)

Tumour resection

5

Yes

CB1002

HR

644 (79%)

105 (13%)

Diagnosis of relapse

5

No

CB1003

HR

54 (7%)

57 (7%)

Neuroblastoma diagnosis + tumour resection

10

Yes

CB1004

HR

104 (13%)

100 (12%)

Tumour resection

3

No

CB1005

HR

132 (16%)

98 (12%)

Tumour resection

5

No

CB1007

LR

487 (60%)

17 (2%)

Neuroblastoma diagnosis

2

No

CB1008

HR

24 (3%)

353 (44%)

Neuroblastoma diagnosis + tumour resection

6

Yes

CB1009

IMR

561 (69%)

1 (>0%)

Neuroblastoma diagnosis + tumour resection

9

No

CB1010

HR

247 (30%)

33 (4%)

Diagnosis of relapse

3

No

  1. HR high-risk, IMR intermediate risk, LR low risk, MNA MYCN amplification.