A genome-wide allelic analysis of neuroblastoma (NB) revealed a previously
undescribed increased incidence of loss of heterozygosity (LOH) on chromoso
me arm 19q13 primarily affecting stages 3 and 4N disease. Further allelic a
nalysis of chromosome 19q13 in a cohort of 116 NE patients using 17 polymor
phic microsatellite markers identified the shortest common region of loss b
etween D19S606 and D19S112 at 19q13.3. In some cases, clonal LOH at 19q13 w
as acquired during the course of disease, and deleted clones remained after
cytotoxic therapy. In multivariant analysis, 19q13 LOH was associated with
overall survival in local-regional International Neuroblastoma Staging Sys
tem stages 1, 2, and 3 patients and was specifically present in tumors at t
he site of recurrence.