A cell lineage tree, or phylogeny, describes the evolutionary history of cells in a biological sample. Reconstructing cell lineage trees for tumor biopsies may shed light on cancer progression and response to treatment; thus the development of fast and accurate methods is of critical importance. Many popular methods assume that mutations occur according to the infinite sites model and that deviations from a perfect phylogeny are due to sequencing error, as data generated by single-cell platforms are notoriously error-prone. To address this issue, sequencing error is modeled, with false positives, false negatives, and missing values being independent and identically distributed across mutations and cells. Here, we consider how to estimate phylogenies under this model using quartets (i.e., unrooted, binary, four-leaf trees), which are implied by mutations being present in two cells and absent from two cells. Our main result is that the most probable quartet identifies the unrooted cell lineage tree; it follows that the most frequent quartet from the input data is a consistent estimator. This leads us to consider how heuristics developed for maximum quartet support supertrees may further enable cell lineage tree reconstruction. Overall, our work connects statistical theory from species phylogenetics to tumor phylogenetics.